Melting point	190.0-191.0 ºC*

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Source	SDS/MSDS Samples
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Synthetic Route

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Name	CAS

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Articles

Peer-Reviewed Papers

An evaluation of the feasibility of using cytogenetic damage as a biomarker for alachlor exposure.A D Kligerman et al.Mutation research, 441(1), 95-101 (1999-05-04) Enzymatic synthesis of 4-amino-3,5-diethylphenyl sulfate, a rodent metabolite of alachlor.S J Logusch et al.Journal of agricultural and food chemistry, 47(5), 2125-2129 (1999-12-20) Ferrocene-based guanidine derivatives: in vitro antimicrobial, DNA binding and docking supported urease inhibition studies.Rukhsana Gul et al.European journal of medicinal chemistry, 85, 438-449 (2014-08-12) Further evidence of an inverted region in proton transfer within the benzophenone/substituted aniline contact radical ion pairs; importance of vibrational reorganization energy.Libby R Heeb et al.The journal of physical chemistry. A, 110(20), 6408-6414 (2006-05-19) Sister chromatid exchanges of human peripheral blood lymphocytes induced by N,N-diethylaniline in vitro.Q Li et al.Mutation research, 395(2-3), 151-157 (1998-02-18) Urinary biomonitoring for alachlor exposure in commercial pesticide applicators by immunoassay.R E Biagini et al.Bulletin of environmental contamination and toxicology, 54(2), 245-250 (1995-02-01) Determination of alachlor and its metabolite 2,6-diethylaniline in microbial culture medium using online microdialysis enriched-sampling coupled to high-performance liquid chromatography.Chi-Zen Chen et al.Journal of agricultural and food chemistry, 59(15), 8078-8085 (2011-06-29) Biodegradation of alachlor by soil streptomycetes.L Durães Sette et al.Applied microbiology and biotechnology, 64(5), 712-717 (2004-01-17) Determination of serum levels of 2,6 diethylaniline in laboratory animal treated with Alachlor.R Galati et al.Anticancer research, 18(2A), 979-982 (1998-06-06) Lack of alachlor induced DNA damage as assayed in rodent liver by the alkaline elution test.M Taningher et al.Toxicology, 85(2-3), 117-122 (1993-12-31) Spectroscopic studies of molecular interactions involving 2,6-diethylaniline and N-ethylaniline donors and iodine as an electron acceptor in different solvents.Tarek M El-Gogary et al.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 66(1), 94-101 (2006-07-04) Metal-enhanced fluorescence exciplex emission.Yongxia Zhang et al.Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 85(1), 134-138 (2011-11-01)

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